How is quality control of the data performed?

How is %CV calculated?

Why do some of your biomarkers have several Uniprot numbers?

How is it determined whether a sample has failed quality control because of operator error or due to some property of the sample?

I see that the same protein can be measured by more than one panel, are these the same assay?

Why would a sample not pass quality control in only one out of several panels run?

Should I dilute my samples before shipping them to Olink?

How many replicates of each sample are analyzed?

Why do the negative control and interplate control samples flag/not pass the quality control (QC)?

We see a rather low detectability for some of the proteins analyzed for our healthy control group, why is that?